[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Samyang Biopharmaceuticals Corporation\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":85},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,41,60],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100628868","a-prospective-clinical-investigation-of-dmfi300-for-treating-nasolabial-folds-100628868",false,"NCT07467239","A Prospective Clinical Investigation of DMFI300 for Treating Nasolabial Folds","A Prospective, Participant- and Evaluator-blinded, Randomized, Controlled, Split-face Clinical Investigation to Evaluate the Performance and Safety of Polycaprolactone 300 (DMFI300) for the Treatment of Nasolabial Folds","Inclusion Criteria:\n\n* Men and women aged 18-70 years.\n* Score of 3 to 4 on the Wrinkle Severity Rating Scale (WSRS) for both nasolabial folds.\n* Willing and able to provide written informed consent.\n* Willing to comply with study procedures and follow-up visits.\n* Willing to refrain from other facial cosmetic procedures affecting the nasolabial folds during the study.\n\nExclusion Criteria:\n\n* Use of antiplatelet agents, vitamin E, or NSAIDs within 2 weeks before screening or planned use within 2 weeks after treatment.\n* History or presence of bleeding disorders.\n* Participation in another clinical investigation within 1 month prior to screening.\n* Pregnant or breastfeeding women, or women planning pregnancy during the study.\n* Women of childbearing potential not using an effective method of contraception.","ALL","18 Years","70 Years",{"count":20,"type":21},30,"ESTIMATED","INTERVENTIONAL",[24],"NA","This is a prospective, randomized, controlled clinical investigation designed to evaluate the performance and safety of DMFI300 for the treatment of nasolabial folds. 30 adult participants will receive treatment with the investigational device and the comparator device using a split-face design. The study will assess wrinkle severity using validated aesthetic evaluation scales, as well as overall safety.",[27],"Nasolabial Folds, Wrinkles","RECRUITING","2026-03-09",{"date":31,"type":32},"2026-03-12","ACTUAL",{"date":34,"type":32},"2026-03-02",{"date":36,"type":21},"2027-05-31",{"name":38,"class":39},"Samyang Biopharmaceuticals Corporation","INDUSTRY",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":48,"targetDuration":4,"studyType":22,"phases":49,"briefSummary":50,"conditions":51,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":52,"lastUpdatePostDateStruct":53,"startDateStruct":55,"completionDateStruct":57,"leadSponsor":59,"locationsCount":40},"100615451","a-prospective-clinical-investigation-of-dmfi150-for-treating-nasolabial-folds-100615451","NCT07292779","A Prospective Clinical Investigation of DMFI150 for Treating Nasolabial Folds","A Prospective, Clinical Investigation to Evaluate the Performance and Safety of DMFI150 for the Treatment of Nasolabial Folds","Inclusion Criteria:\n\n* Men and women aged 18-70 years.\n* Score of 3 to 4 on the WSRS (1 = absent, 2 = mild, 3 = moderate, 4 = severe, and 5 = extreme) for both nasolabial folds.\n* Able and willing to provide written informed consent.\n* Willing to refrain from facial cosmetic procedures during the study.\n\nExclusion Criteria:\n\n* Use of antiplatelet agents, vitamin E, or NSAIDs within 2 weeks before screening or 2 weeks after treatment.\n* History or current bleeding disorders.\n* Participation in another clinical trial within 1 month before screening.\n* Pregnant or breastfeeding women, or planning pregnancy.\n* Women of childbearing potential not using effective contraception.",{"count":20,"type":21},[24],"This is a prospective clinical investigation designed to evaluate the performance and safety of DMFI150 for the treatment of nasolabial folds. 30 adult participants will receive a single treatment with the investigational device. The study will assess wrinkle severity using validated aesthetic evaluation scales, as well as overall safety.",[27],"2026-03-04",{"date":54,"type":32},"2026-03-05",{"date":56,"type":32},"2025-11-24",{"date":58,"type":21},"2026-12",{"name":38,"class":39},{"id":61,"slug":62,"hasResults":11,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":4,"eligibilityCriteria":66,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":67,"targetDuration":4,"studyType":22,"phases":69,"briefSummary":70,"conditions":71,"keywords":73,"overallStatus":76,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":4},"100589979","a-study-in-adults-evaluating-polycaprolactone-microsphere-filler-for-treatment-of-moderate-to-severe-nasolabial-folds-100589979","NCT06961448","A Study in Adults Evaluating Polycaprolactone Microsphere Filler for Treatment of Moderate to Severe Nasolabial Folds","A Prospective, Multi-center, Evaluator-blinded, Randomized, Parallel-controlled, Superiority Clinical Trial to Evaluate the Safety and Efficacy of Polycaprolactone Microsphere Fillers for Correction of Moderate to Severe Nasolabial Folds","Inclusion Criteria:\n\n1. Aged 18 or above, with no gender restriction.\n2. Willing to receive treatment for correcting nasolabial fold.\n3. Treatment investigator evaluate those with a WSRS score of 3 or 4 for bilateral nasolabial folds;\n4. Willing to voluntarily participate in the clinical trial, accepting the obligation not toreceive all plastic surgery and cosmetic dermatology procedures or treatments during the trial。 Willing and able to undergo the required treatment and follow-up observations, and sign the informed consent form.\n\nExclusion Criteria:\n\n1. Allergy to polycaprolactone, hyaluronic acid products or any component of the investigational device or control device(such as streptococcal proteins), allergy to any local anesthetic (such as lidocaine or other amide-typeanesthetic), or history of severe allergic reactions and multiple severe allergic reactions.\n2. Previous surgery, cosmetic facial procedure, or plans to undergo cosmetic surgery in NLF area or lower face during the trial, inculding any of the following circumstances:\n\n   1. Received permanent fillers or prostheses (such as PMMA etc.) or semi-permanent dermal fillers (such as CaHA, PLLA, PCL, etc.).\n   2. Received temporary dermal fillers (such as HA and collagen etc.) within 12 months prior to screening.\n   3. Received anti-wrinkle surgery within 12 months prior to screening.\n   4. Receiving botulinum toxin injection, chemical stripping, radiofrequency laser, and liquid nitrogen freezing anti-wrinkle treatment within 6 months.\n3. Individuals who used topical agents (e.g., corticosteroids, steroids \\[excluding hydrocortisone\\], retinoids, or retinoid derivatives intended as medications but not as cosmetics) on the mid-to-lower facial area within 3 months prior to screening or plan to use them during the trial period, as well as those undergoing hydrocortisone treatment.\n4. Individuals with abnormal coagulation mechanisms \\[activated partial thromboplastin time (APTT) \\>1.5 times the upper limit of normal (ULN), etc.\\], or use of anticoagulants (e.g., warfarin, rivaroxaban), antiplatelet agents (e.g., aspirin, clopidogrel), thrombolytic agents (e.g., recombinant human urokinase) within 2 weeks prior to screening.\n5. Individuals with severe liver or kidney dysfunction, such as liver function markers (ALT, AST) exceeding 2 times the ULN or kidney function markers (creatinine) exceeding 1.5 times the ULN.\n6. Individuals with infectious diseases, including any positive test results for hepatitis B surface antigen, hepatitis C antibodies, HIV antibodies, or syphilis antibodies.\n7. Individuals with scars, unhealed wounds, deformities, defects, tattoos, or excessive pigmentation in the nasolabial fold area that may affect the efficacy assessment.\n8. Individuals with tumors, precancerous lesions, active skin lesions such as herpes, in the nasolabial fold area.\n9. Individuals with acute or chronic skin diseases such as infections or inflammation in the treatment area.\n10. Individuals with autoimmune diseases, such as psoriasis.\n11. Individuals with uncontrolled diabetets.\n12. Individuals prone to scarring, keloid formation, or hypertrophic scars.\n13. Individuals diagnosed with psychiatric disorders, lacking self-autonomy, or experiencing active episodes of anxiety or depression.\n14. Individuals with excessively high expectations of treatment outcomes or unwilling to accept potential short-term side effects such as bruising, swelling, or pain.\n15. Individuals who are pregnant, breastfeeding, or unwilling to use medically approved contraception (e.g., oral contraceptives, condoms, intrauterine devices) during the trial.\n16. Individuals who participated in other drug or medical device clinical trials within 3 months prior to screening.\n17. Individuals deemed unsuitable for trial participation by the investigator for other reasons.",{"count":68,"type":21},208,[24],"The goal of this clinical trial is to evaluate the safety and efficacy of polycaprolactone microsphere filler (Lafullen) for the correction of moderate to severe nasolabial folds in adults aged 18 and above, regardless of gender.\n\nThe main questions it aims to answer are:\n\n* Does Lafullen improve wrinkle severity in the nasolabial fold area at 48 weeks post-injection (WSRS responder rate)?\n* Is Lafullen superior to the control product (Restylane, a hyaluronic acid filler) in terms of long-term wrinkle correction and safety? Researchers will compare Lafullen (polycaprolactone filler) with Restylane (modified sodium hyaluronate gel) to see if Lafullen provides superior wrinkle correction at 12 months post-injection.\n\nParticipants will:\n\n* Receive either Lafullen or Restylane via injection in the nasolabial fold area.\n* Optionally receive a touch-up injection at 4 weeks after the first treatment if needed.\n* Undergo regular follow-up visits at 4, 12, 24, 36, and 48 weeks post-treatment.\n* Subjects in the Lafullen group will continue follow-up up to 72 weeks to assess long-term efficacy and safety.\n* Be assessed through clinical photography, pain scale (VAS), satisfaction questionnaires, and safety evaluations (e.g., AEs, vital signs, lab tests).",[72],"Nasolabial Fold Correction",[74,75],"Polycaprolactone microsphere filler","Nasolabial folds","NOT_YET_RECRUITING","2025-04-29",{"date":79,"type":32},"2025-05-08",{"date":81,"type":21},"2025-05-01",{"date":83,"type":21},"2026-11-01",{"name":38,"class":39},""]